基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Clinicopathological features associated with CD44 and CD63 expression in breast cancer.
Clinicopathological features associated with CD44 and CD63 expression in breast cancer.
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CD44 表达与侵袭性特征及低 CD63 密度染色相关。
CD44 是一种细胞表面跨膜糖蛋白,参与调节多种细胞过程,包括细胞分裂、黏附、迁移和干细胞样特征。CD63 参与胞吐过程。
评估 CD44 和 CD63 表达与临床病理特征(包括TIL(肿瘤浸润淋巴细胞)[TIL])、磷脂酰肌醇 3-激酶(PIK3CA)突变和生存之间的关系。
对 101 例秘鲁女性乳腺癌患者样本进行 CD44 和 CD63 染色。
年龄中位数为 52 岁,多数患者为 3 级肿瘤(68%)、雌激素受体(ER)阳性(64%)和 II–III 期(92%)。Ki-67 中位数为 30%,间质 TIL 中位数为 30%,49% 患者存在 PIK3CA 突变。较长生存与早期分期(p = 0.016)、Ki-67 较低(p = 0.023)、ER 阳性(p = 0.034)、管腔型表型(p = 0.029)和复发(p < 0.001)相关。57% 病例 CD44 染色细胞密度高,55% 染色强度高。CD44 高密度与年龄较轻(p = 0.043)、三阴性表型(p = 0.035)和较短生存(p = 0.005)相关。CD44 高表达也与生存期短相关(p = 0.005)。56% 病例 CD63 细胞密度高,且与 ER 阳性(p = 0.045)、TIL 水平低(p = 0.007)、管腔 A 型(p = 0.015)和 CD44 染色强度低(p = 0.032)相关。
CD44 表达与侵袭性特征以及 CD63 染色密度低相关。
CD44 is a cell-surface transmembrane glycoprotein that participates in the regulation of many cellular processes, including cell division, adhesion, migration and stem-like characteristics. CD63 is involved in the exocytosis process.
To evaluate the relationship between CD44 and CD63 expression and clinicopathological features, including tumor-infiltrating lymphocytes (TILs), phosphoinositide 3-kinase (PIK3CA) mutation and survival. METHODOLOGY: CD44 and CD63 were stained in samples from 101 breast cancer cases from Peruvian women.
Median age was 52 years, most were most were grade-3 (68%), estrogen receptor (ER)+ (64%) and stage II-III (92%). Median ki67 was 30%, median stromal TIL was 30% and PIK3CA mutation was found in 49%. Longer survival was associated with earlier stages ( p = 0.016), lower ki67 ( p = 0.023), ER+ ( p = 0.034), luminal phenotype ( p = 0.029) and recurrence ( p < 0.001). CD44 was classified as high cell density staining in 57% and high intensity in 55%. High CD44 density was associated with younger age ( p = 0.043), triple-negative phenotype ( p = 0.035) and shorter survival ( p = 0.005). High CD44 expression was associated with short survival ( p = 0.005). High CD63 cell density was found in 56% of cases and was associated with ER-positive ( p = 0.045), low TIL levels ( p = 0.007), Luminal-A ( p = 0.015) and low CD44 intensity ( p = 0.032).
CD44 expression was associated with aggressive features and low CD63 density staining.
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